Showing entry for BRACHYDACTYLY, TYPE A1 (disorder)



                               
General Disease Information
BXGD IdBXGD016110
Disease NameBRACHYDACTYLY, TYPE A1 (disorder)
Disease CUI IdC1862151
MeSH Codes C16   C05  
Disease Class NameCongenital, Hereditary, and Neonatal Diseases and Abnormalities; Musculoskeletal Diseases
Semantic TypeDisease or Syndrome
Human Phenotype Ontology Id HP:0040064   HP:0000924  
Human Phenotype Ontology TermAbnormality of limbs; Abnormality of the skeletal system
Disease Ontology Id DOID:630   DOID:7  
Disease Ontology Class Namegenetic disease; disease of anatomical entity
Disorder Network disorder-protein-compound-food associations